Taiwan FDA registration 4ec779e84e6e8be4ffd0a3c1f1322bca
"Lifetech Technologies" Coleus ventricular middle diaphragm defect occluder
TW: "先健科技公司"寇納心室中膈缺損封堵器
Taiwan·Risk Class 3·LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD·Registered Mar 04, 2021 – Mar 04, 2026ExpiredRegistration details
- Analysis ID
- 4ec779e84e6e8be4ffd0a3c1f1322bca
- Customs Code
- DHA09200120506
Company information
- Manufacturer
- LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- KAISEN MEDICAL CO., LTD
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.9999 Miscellaneous
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 04, 2021
- Expiry Date
- Mar 04, 2026
About this record
Access comprehensive regulatory information for "Lifetech Technologies" Coleus ventricular middle diaphragm defect occluder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4ec779e84e6e8be4ffd0a3c1f1322bca and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices